Formaldehyde → N-Methylleucine

HRID 1089821

Reaktionsgleichung

Reaktionsgleichung von HRID 1089821
C1C2C(CO[C:16]([NH:18][C@H:19]([C:24]([OH:26])=[O:25])[CH2:20][CH:21]([CH3:23])[CH3:22])=O)C3C(=CC=CC=3)C=2C=CC=1.C=O.FC(F)(F)C(O)=O.C([SiH](CC)CC)C>C1(C)C=CC=CC=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>[CH3:16][NH:18][C@H:19]([C:24]([OH:26])=[O:25])[CH2:20][CH:21]([CH3:23])[CH3:22]

Komponenten

7

Versuchsvorschrift

A suspension of N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-leucine (1.67 g, 5 mmol) in toluene(100 ml) was charged with paraformaldehyde (1 g, 33.3 mmol) and 4-toluenesulfonic acid (100 mg, catalytic). The mixture was refluxed for 30 minutes in a Dean Stark apparatus for azeotropic distillation. The solution was washed with a saturated solution of sodium bicarbonate (×2), dried over magnesium sulfate and evaporated. The resulting oil in a 1:1 mixture of chloroform:trifluoroacetic acid (50 ml), at room temperature, was charged with triethylsilane (2.38 ml, 15 mmol). Stirring was continued for 22 hr. The solvents were removed in vacuum and the oil was crystallized from a mixture of ether:hexane. Recrystalyzation from EtOAc:hexane afforded 0.85 g (46%) of the product as a colorless solid, mp 101°-3° C.

Aufarbeitung

  1. temperatureThe mixture was refluxed for 30 minutes in a Dean Stark apparatus for azeotropic distillation
  2. washThe solution was washed with a saturated solution of sodium bicarbonate (×2)
  3. dry with materialdried over magnesium sulfate
  4. customevaporated
  5. additionThe resulting oil in a 1:1 mixture of chloroform
  6. customThe solvents were removed in vacuum
  7. customthe oil was crystallized from a mixture of ether

Quellen und Nachweise

ORD-Eintrag
ord-53ad8a2361374f15a4ed27622a2ceb26
Quelldatensatz
uspto-grants-1992_01
Patentnummer
US05079260

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